Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Maria Rita Carriero"'
Autor:
Francesca Lazzaroni, Jennifer M.T.A. Meessen, Ying Sun, Silvia Lanfranconi, Elisa Scola, Quintino Giorgio D'Alessandris, Laura Tassi, Maria Rita Carriero, Marco Castori, Silvia Marino, Adriana Blanda, Enrico B. Nicolis, Deborah Novelli, Roberta Calabrese, Nicolò M. Agnelli, Barbara Bottazzi, Roberto Leone, Selene Mazzola, Silvia Besana, Carlotta Catozzi, Luigi Nezi, Maria G. Lampugnani, Matteo Malinverno, Nastasja Grdseloff, Claudia J. Rödel, Behnam Rezai Jahromi, Niccolò Bolli, Francesco Passamonti, Peetra U. Magnusson, Salim Abdelilah-Seyfried, Elisabetta Dejana, Roberto Latini
Publikováno v:
EBioMedicine, Vol 99, Iss , Pp 104914- (2024)
Summary: Background: Cerebral Cavernous Malformation (CCM) is a rare cerebrovascular disease, characterized by the presence of multiple vascular malformations that may result in intracerebral hemorrhages (ICHs), seizure(s), or focal neurological defi
Externí odkaz:
https://doaj.org/article/5d07c7a73f1a46f0b5225cf9e0e0aa36
Autor:
Silvia Lanfranconi, Elisa Scola, Giulio Andrea Bertani, Barbara Zarino, Roberto Pallini, Giorgio d’Alessandris, Emanuela Mazzon, Silvia Marino, Maria Rita Carriero, Emma Scelzo, Giuseppe Faragò, Marco Castori, Carmela Fusco, Antonio Petracca, Leonardo d’Agruma, Laura Tassi, Piergiorgio d’Orio, Maria Grazia Lampugnani, Enrico Bjorn Nicolis, Antonella Vasamì, Deborah Novelli, Valter Torri, Jennifer Marie Theresia Anna Meessen, Rustam Al-Shahi Salman, Elisabetta Dejana, Roberto Latini, the Treat-CCM Investigators
Publikováno v:
Trials, Vol 21, Iss 1, Pp 1-10 (2020)
Abstract Background Cerebral cavernous malformations (CCMs) are vascular malformations characterized by clusters of enlarged leaky capillaries in the central nervous system. They may result in intracranial haemorrhage, epileptic seizure(s), or focal
Externí odkaz:
https://doaj.org/article/f05152bef83d4a7394e2bd682275786c
Autor:
Maria Grazia Bruzzone, Fabio Longaretti, F. Ghielmetti, Fady T. Charbel, Elisa Ciceri, Luigi Caputi, Gian Paolo Anzola, Maria Rita Carriero, Eugenio Parati, Giuseppe Faragò, Massimo Lamperti
Publikováno v:
European Journal of Radiology. 83:1005-1010
Assessment of cerebrovascular reactivity (CVR) is essential in cerebrovascular diseases, as exhausted CVR may enhance the risk of cerebral ischemic events. Transcranial Doppler (TCD) with a vasodilatory stimulus is currently used for CVR evaluation.
Autor:
Steven M. Greenberg, Luisa Chiapparini, Giuseppe Billo, Fabrizio Tagliavini, Jacopo C. DiFrancesco, Fabrizio Piazza, Carlo Ferrarese, Giuseppe Piscosquito, Giorgio Giaccone, M. Brioschi, Maria Rita Carriero, Antonio Colombo, Margherita Gardinetti, Mario Savoiardo, Hideya Sakaguchi, Ricardo Nitrini, Irina Raicher, Francesca Lanzani
Publikováno v:
Annals of Neurology. 73:449-458
Objective Cerebral amyloid angiopathy–related inflammation (CAA-ri) is characterized by vasogenic edema and multiple cortical/subcortical microbleeds, sharing several aspects with the recently defined amyloid-related imaging abnormalities (ARIA) re
Autor:
Fabrizio Piazza, Margherita Gardinetti, Luisa Chiapparini, Jacopo C. DiFrancesco, Fabrizio Tagliavini, Maria Rita Carriero, Mario Savoiardo, M. Brioschi, Giuseppe Piscosquito, Irina Raicher, Giuseppe Billo, Francesca Lanzani, Antonio Colombo, Hideya Sakaguchi, Carlo Ferrarese, Giorgio Giaccone, Steven M. Greenberg
Publikováno v:
Journal of Neuroimmunology
Autor:
Chiara Falcone, Gennaro Bussone, Domenico D'Amico, Susanna Usai, Luigi Caputi, Gian Paolo Anzola, Maria Rita Carriero, Licia Grazzi, Eugenio Parati, Massimo Del Sette
Publikováno v:
Headache: The Journal of Head and Face Pain. 50:1320-1327
(Headache 2010;50:1320-1327) Background.— There is a well-known association between migraine with aura (MA) and right-to-left shunt (RILES) because of patent foramen ovale (PFO). The occurrence of MA attacks after microbubble (MB) injection during
Autor:
Elena Corsini, Carla Brambilla, Giorgio B. Boncoraglio, Antonella Bodini, Maria Rita Carriero, Eugenio Parati
Publikováno v:
Clinical neurology and neurosurgery (Dutch-Flem. ed.) 111 (2009): 270–273. doi:10.1016/j.clineuro.2008.11.001
info:cnr-pdr/source/autori:Boncoraglio G.; Bodini A.; Brambilla C.; Corsini E.; Carriero MR.; Parati E.A./titolo:Aspirin resistence determined with PFA-100 does not predict thrombotic events in patients with stable ischemic cerebrovascular disease/doi:10.1016%2Fj.clineuro.2008.11.001/rivista:Clinical neurology and neurosurgery (Dutch-Flem. ed.)/anno:2009/pagina_da:270/pagina_a:273/intervallo_pagine:270–273/volume:111
info:cnr-pdr/source/autori:Boncoraglio G.; Bodini A.; Brambilla C.; Corsini E.; Carriero MR.; Parati E.A./titolo:Aspirin resistence determined with PFA-100 does not predict thrombotic events in patients with stable ischemic cerebrovascular disease/doi:10.1016%2Fj.clineuro.2008.11.001/rivista:Clinical neurology and neurosurgery (Dutch-Flem. ed.)/anno:2009/pagina_da:270/pagina_a:273/intervallo_pagine:270–273/volume:111
Objective Evidence is growing that some patients are not responsive to the antithrombotic action of aspirin. We prospectively evaluated the ability of aspirin resistance status, determined by PFA-100, to predict new thrombotic events in patients with
Autor:
Isabella Ceccherini, Grazietta Gattellaro, Roberto Fancellu, Andrea Salmaggi, Laura Farina, Maria Rita Carriero, Caterina Mariotti, Francesco Carella, Silvia Romano, Davide Pareyson, Floriano Girotti, Mario Savoiardo
Publikováno v:
Brain. 131:2321-2331
Alexander disease (AD) in its typical form is an infantile lethal leucodystrophy, characterized pathologically by Rosenthal fibre accumulation. Following the identification of glial fibrillary acidic protein (GFAP) gene as the causative gene, cases o
Autor:
Giorgio B. Boncoraglio, Emilio Ciusani, Carla Brambilla, Maria Rita Carriero, Eugenio Parati, Antonella Bodini
Publikováno v:
Cerebrovascular diseases (Basel) 22 (2006): 191–195. doi:10.1159/000093604
info:cnr-pdr/source/autori:Boncoraglio G.B.; Bodini A.; Brambilla C.; Carriero M.R.; Ciusani E.; Parati E.A./titolo:An effect of PAI-1 4G%2F5G polymorphism on cholesterol levels may explain conflicting associations with myocardial infarction and stroke/doi:10.1159%2F000093604/rivista:Cerebrovascular diseases (Basel)/anno:2006/pagina_da:191/pagina_a:195/intervallo_pagine:191–195/volume:22
info:cnr-pdr/source/autori:Boncoraglio G.B.; Bodini A.; Brambilla C.; Carriero M.R.; Ciusani E.; Parati E.A./titolo:An effect of PAI-1 4G%2F5G polymorphism on cholesterol levels may explain conflicting associations with myocardial infarction and stroke/doi:10.1159%2F000093604/rivista:Cerebrovascular diseases (Basel)/anno:2006/pagina_da:191/pagina_a:195/intervallo_pagine:191–195/volume:22
Background and Purpose:The gene-encoding plasminogen activator inhibitor type 1 (PAI-1) has a common 4G/5G ‘functional’ polymorphism, and people homozygous for the 4G allele have higher PAI-1 plasma concentrations. The 4G/4G genotype is associate
Autor:
Emilio Ciusani, Maria Rita Carriero, Eugenio Parati, Luisa Chiapparini, Giorgio B. Boncoraglio, Alessandra Erbetta, E. Ciceri
Publikováno v:
European Journal of Neurology. 11:405-409
Despite the continuous description of new conditions pre-disposing for cerebral venous thrombosis (CVT), no apparent cause is found in about 30% of cases. Hyperhomocysteinemia (hyper-Hcy) is an established risk factor for deep venous thrombosis and s